ClinVar Miner

Submissions for variant NM_019074.4(DLL4):c.1074T>C (p.His358=)

gnomAD frequency: 0.01647  dbSNP: rs28568593
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000971304 SCV001118943 benign not provided 2025-01-18 criteria provided, single submitter clinical testing
GeneDx RCV000971304 SCV001947356 benign not provided 2020-05-18 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000971304 SCV005296843 benign not provided criteria provided, single submitter not provided

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